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Abstract
Leishmania tropica causes different forms of leishmaniasis in many parts of the
world. Animal models can help to clarify the issues of pathology and immune
response in L. tropica infections and can be applied to the control, prevention and
treatment of the disease. The aim of this article is to summarize published data related
to experimental models of this parasite, presenting an overview of the subject. We
also present in brief the epidemiology, transmission and human manifestation of L.
tropica infection.
Mice, rats and hamsters have been used for experimental models of L.
tropica infection. Main findings of the published studies show that: (1) Hamsters are
the best animal model for L. tropica infection, with the drawback of being outbred
hence not suitable for many studies. (2) L. tropica infection causes a non-ulcerative
and chronic pathology as cutaneous form in mice and usually visceral form in
hamsters. (3) L. tropica infection in mice results in a weaker immune response in
comparison to Leishmania major. (4) While the Th1 responses are evoked against L.
tropica, Th2 responses do not explain the outcomes of this infection, and IL-10
and TGF-β are two main suppressive cytokines. (5) The host genotype affects the
immune response and disease outcome of L. tropica infection and the dose, strain,
routes of inoculation, and sex of the host are among the factors affecting disease
outcome of this species.
Epidemiology
Leishmania tropica is endemic to those countries of Europe and northern Africa
bordering the Mediterranean Sea and to the Asian countries of Syria, Israel, southern
Russia, China, Vietnam, and India. L. mexicana has been reported from Peru, Bolivia,
Brazil, the Guianas, and Mexico. A variant clinical form of cutaneous leishmaniasis
occurring in South and Central America and Ethiopia is referred to as diffuse
cutaneous leishmaniasis (DCL). DCL never heals spontaneously and there is a
tendency to relapse after treatment.
The vectors for L. tropica and L. mexicana are members of the sandfly
genera Phlebotomus and Lutzomyia, respectively. The life cycles of L. tropica and L.
mexicana parallel that of L. donovani. In addition to humans, L. tropica infects dogs
and cats in China and a few Mediterranean countries. Natural infections are known to
occur in monkeys, bullocks, and brown bears in the Middle East, as well as horses and
gerbils. In some areas of the Middle East, the infection is endemic among rodents in
whose burrows the sandflies live and breed. Humans, intruding in these areas, are
readily infected. A few instances of L. tropica infecting the spleen and lymph glands
(viscerotropic infection) have been reported in American military personnel in the
Middle East following the Persian Gulf War (1990-91). In the Western Hemisphere,
dogs serve as the primary domestic reservoir, while armadillos and arboreal rodents
may also serve as sylvatic reservoirs.
(Alan J Magill, in Hunter's Tropical Medicine and Emerging Infectious Disease
(Ninth Edition), 2013)
In the midgut of the sand-fly, the amastigotes develop into promastigotes which
replicate profusely. These are, in turn, transmitted to the skin of persons bitten by the
sandflies.
(https://www.notesonzoology.com/parasitology/leishmania-tropica-morphology-and-
pathogenicity-zoology/4671)